PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
26852716-5	2016	Further, binding locations and dissociation constants obtained for both benzocaine (660 muM) and phenytoin (1 muM) in the mutant channels were within the range expected from experimental values obtained from drug binding to eukaryotic sodium channels, indicating that these mutant NavAb may be a better model for drug binding to eukaryotic channels than the wild type.	Phenytoin	97-106	latexin	Homo sapiens	110-113	
28160766-4	2017	After 48 h of 0.25 muM PHT treatment, appearance of apoptotic cells was detected by TUNEL assay.	Phenytoin	23-26	latexin	Homo sapiens	19-22	
4505652-1	1972	Diphenylhydantoin, in concentration of 5-50 muM, decreases the early, transient (sodium) currents of voltage-clamped squid giant axons.	Phenytoin	0-17	latexin	Homo sapiens	44-47	
30841439-4	2019	Treatments of T84 cell monolayers with specific CAR agonists (CITCO and phenytoin at concentrations of 1 muM and 5 muM, respectively) for 24 h decreased transepithelial Cl- secretion in response to cAMP-dependent agonist.	Phenytoin	72-81	latexin	Homo sapiens	105-108	
30841439-4	2019	Treatments of T84 cell monolayers with specific CAR agonists (CITCO and phenytoin at concentrations of 1 muM and 5 muM, respectively) for 24 h decreased transepithelial Cl- secretion in response to cAMP-dependent agonist.	Phenytoin	72-81	latexin	Homo sapiens	115-118	
22157126-5	2012	TTX (0.2 muM) or phenytoin (50 muM) terminated ictal-like events, suggesting that the persistent Na(+) current (I(NaP)) is pivotal for type I behavior.	Phenytoin	17-26	latexin	Homo sapiens	31-34